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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5469067copy number variation1nstd206human GRCh38 chr5: 79,000,348-79,000,414 , GRCh37.p13 chr5: 78,296,171-78,296,237 DMGDH, LOC100505796
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4675682copy number variation1nstd102humanUncertain significance GRCh37 chr5: 78,094,810-78,936,391 , GRCh38.p12 chr5: 78,798,987-79,640,568 LOC107986426, ARSB, 14 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4456838copy number variation1nstd102humanUncertain significance GRCh37 chr5: 78,229,182-78,844,914 , GRCh38.p12 chr5: 78,933,359-79,549,091 BHMT2, LOC102724530, 13 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv3922603copy number variation1nstd102humanUncertain significance NCBI36 chr5: 78,135,940-78,951,758 , GRCh38 chr5: 78,804,361-79,620,179 , GRCh37 chr5: 78,100,184-78,916,002 BHMT2, LOC105379047, 14 more genes
    nsv3917856copy number variation1nstd102humanPathogenic GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153 CSNK1A1P3, POLR3G, 413 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3877842copy number variation1nstd102humanBenign GRCh37 chr5: 78,265,041-78,558,425 , GRCh38.p12 chr5: 78,969,218-79,262,602 BHMT2, JMY, 5 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv3137223copy number variation1nstd151human GRCh37 chr5: 78,077,672-78,301,235 , GRCh38.p12 chr5: 78,781,849-79,005,412 LOC100505796, ARSB, 1 more genes
    nsv3133417copy number variation2nstd151human GRCh37 chr5: 78,251,115-78,752,846 , GRCh38.p12 chr5: 78,955,292-79,457,023 LOC101929201, RPS3AP20, 9 more genes
    nsv3129176copy number variation1nstd151human GRCh37 chr5: 78,111,906-78,938,738 , GRCh38.p12 chr5: 78,816,083-79,642,915 LOC102724530, BHMT, 14 more genes
    nsv3123749copy number variation1nstd151human GRCh37 chr5: 78,264,826-78,426,944 , GRCh38.p12 chr5: 78,969,003-79,131,121 LOC100505796, ARSB, 3 more genes
    nsv2345079short tandem repeat1nstd128human GRCh37 chr5: 78,295,935-78,295,949 , GRCh38.p12 chr5: 79,000,112-79,000,126 DMGDH, LOC100505796
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